nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A case of hypertensive encephalopathy with extensive spinal lesions on MRI
|
Nagato, Masako |
|
2010 |
32 |
7 |
p. 598-601 4 p. |
artikel |
2 |
Announcement: JSCN Best Paper Awards
|
|
|
2010 |
32 |
7 |
p. I- 1 p. |
artikel |
3 |
Announcements and reports
|
|
|
2010 |
32 |
7 |
p. II-VI nvt p. |
artikel |
4 |
Bilateral brachial plexus palsy and right Horner syndrome due to congenital cervicothoracal syringomyelia
|
Çağan, Eren |
|
2010 |
32 |
7 |
p. 595-597 3 p. |
artikel |
5 |
Cognitive evolution of a girl submitted to right hemispherotomy when five years old
|
Vigliano, Piernanda |
|
2010 |
32 |
7 |
p. 579-582 4 p. |
artikel |
6 |
Contents
|
|
|
2010 |
32 |
7 |
p. IBC- 1 p. |
artikel |
7 |
Editorial Board
|
|
|
2010 |
32 |
7 |
p. IFC- 1 p. |
artikel |
8 |
Effects of stress of postnatal development on corticosterone, serotonin and behavioral changes
|
Matsui, Fumihiro |
|
2010 |
32 |
7 |
p. 517-523 7 p. |
artikel |
9 |
Functional deficiencies of sulfite oxidase: Differential diagnoses in neonates presenting with intractable seizures and cystic encephalomalacia
|
Sass, Jörn Oliver |
|
2010 |
32 |
7 |
p. 544-549 6 p. |
artikel |
10 |
Guide for Authors
|
|
|
2010 |
32 |
7 |
p. VII-XI nvt p. |
artikel |
11 |
Hereditary spastic paraplegia and axonal motor neuropathy caused by a novel SPG3A de novo mutation
|
Fusco, Carlo |
|
2010 |
32 |
7 |
p. 592-594 3 p. |
artikel |
12 |
Hypomyelination, hypogonadotropic hypogonadism, hypodontia – First Polish patient
|
Bekiesinska-Figatowska, Monika |
|
2010 |
32 |
7 |
p. 574-578 5 p. |
artikel |
13 |
Non-convulsive status epilepticus and audiogenic seizures complicating a patient with asymmetrical epileptic spasms
|
Saito, Yoshiaki |
|
2010 |
32 |
7 |
p. 583-587 5 p. |
artikel |
14 |
Parieto-occipital encephalomalacia in neonatal hyperammonemia with ornithine transcarbamylase deficiency: A case report
|
Okanishi, Tohru |
|
2010 |
32 |
7 |
p. 567-570 4 p. |
artikel |
15 |
Pontine hypoplasia in 5p-syndrome: A key MRI finding for a diagnosis
|
Ninchoji, Takeshi |
|
2010 |
32 |
7 |
p. 571-573 3 p. |
artikel |
16 |
Positive association between benign familial infantile convulsions and LGI4
|
Ishii, Atsushi |
|
2010 |
32 |
7 |
p. 538-543 6 p. |
artikel |
17 |
Recurrent acute cerebellar ataxia associated with anti-cardiolipin antibodies
|
Ishikawa, Nobutsune |
|
2010 |
32 |
7 |
p. 588-591 4 p. |
artikel |
18 |
Structural basis of neuronal ceroid lipofuscinosis 1
|
Ohno, Kazuki |
|
2010 |
32 |
7 |
p. 524-530 7 p. |
artikel |
19 |
The syndrome of perisylvian polymicrogyria with congenital arthrogryposis
|
Poduri, Annapurna |
|
2010 |
32 |
7 |
p. 550-555 6 p. |
artikel |
20 |
Thiamine-deficient encephalopathy due to excessive intake of isotonic drink or overstrict diet therapy in Japanese children
|
Saeki, Keisuke |
|
2010 |
32 |
7 |
p. 556-563 8 p. |
artikel |
21 |
Transiently reduced water diffusion in the corpus callosum in infants with benign partial epilepsy in infancy
|
Okumura, Akihisa |
|
2010 |
32 |
7 |
p. 564-566 3 p. |
artikel |
22 |
Voxel-based analysis of white matter during adolescence and young adulthood
|
Qiu, Mingguo |
|
2010 |
32 |
7 |
p. 531-537 7 p. |
artikel |